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WGU D115 Advanced Pathophysiology Exam Study Guide with complete solutions | Latest 2025/2026 Update.

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Vista previa 4 fuera de 41 páginas

What causes Marfan's syndrome? Defects or deletions (pathogenic variants) of the fibrillin-1 (FBN1) gene have been shown to cause Marfans syndrome at least 25% of Marfan syndrome cases result from a new mutation in the FBN1 gene spina bifida a congenital defect that occurs during early pregnancy when the spinal canal fails to close completely around the spinal cord to protect it What can cause Spina Bifida Decreased folic acid or maternal use of valproic acid Turner syndrome characteristics Underdeveloped ovaries (sterile) Short stature (~ 4'7") Webbing of the neck Edema Underdeveloped breasts; wide nipples High number of aborted fetuses Diagnostic testing for Turner's syndrome genetic testing , echo, bone density, and bone age testing are necessary. Treatment of Turners syndrome Treatment involves estrogen therapy and growth hormone administration. Treat symptomatically for all other effects of the dz. Cushing's Syndrome a condition caused by prolonged exposure to high levels of cortisol Cushing syndrome symptoms fatty hump between shoulders, a rounded face(moon faced), and pink or purple stretch marks on skin, thinning fragile skin, slow healing of cuts, insect bites and infections, acne, decreased libido, decreased fertility, irregular or absent menstrual periods, fatigue, muscle weakness, cognitive difficulties, and headaches. Turner Syndrome A chromosomal disorder in females in which either an X chromosome is missing, making the person XO instead of XX, or part of one X chromosome is deleted.

Vista previa del contenido

WGU D115 Advanced Pathophysiology i,- i,- i,- i,-




Exam Study Guide with complete i,- i,- i,- i,- i,-




solutions | Latest 2025/2026 Update. i,- i,- i,- i,-




What causes Marfan's syndrome?
i,- Defects or deletions
i,- i,- i,-i,- i,- i,- i,- i,-



(pathogenic variants) of the fibrillin-1 (FBN1) gene have been
i,- i,- i,- i,- i,- i,- i,- i,- i,-



shown to cause Marfans syndrome
i,- i,- i,- i,-




at least 25% of Marfan syndrome cases result from a new
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



mutation in the FBN1 gene i,- i,- i,- i,-




spina bifida i,-a congenital defect that occurs during early
i,-i,- i,- i,- i,- i,- i,- i,- i,- i,-



pregnancy when the spinal canal fails to close completely around
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



the spinal cord to protect it
i,- i,- i,- i,- i,-




What can cause Spina Bifida
i,- i,- i,- i,- i,-i,- i,- Decreased folic acid or maternal i,- i,- i,- i,- i,-



use of valproic acid
i,- i,- i,-




Turner syndrome characteristics
i,- i,- i,-i,- i,- Underdeveloped ovaries i,- i,-



(sterile)
Short stature (~ 4'7")
i,- i,- i,-




Webbing of the neck i,- i,- i,-

,Edema
Underdeveloped breasts; wide nipples i,- i,- i,- i,-




High number of aborted fetuses
i,- i,- i,- i,-




Diagnostic testing for Turner's syndrome genetic testing ,
i,- i,- i,- i,- i,-i,- i,- i,- i,- i,-



echo, bone density, and bone age testing are necessary.
i,- i,- i,- i,- i,- i,- i,- i,-




Treatment of Turners syndrome Treatment involves estrogen
i,- i,- i,- i,-i,- i,- i,- i,- i,-



therapy and growth hormone administration. Treat
i,- i,- i,- i,- i,- i,-



symptomatically for all other effects of the dz. i,- i,- i,- i,- i,- i,- i,-




Cushing's Syndrome a condition caused by prolonged
i,- i,-i,- i,- i,- i,- i,- i,- i,-



exposure to high levels of cortisol i,- i,- i,- i,- i,-




Cushing syndrome symptoms i,- fatty hump between shoulders, i,- i,-i,- i,- i,- i,- i,- i,-



a rounded face(moon faced), and pink or purple stretch marks on
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



skin, thinning fragile skin, slow healing of cuts, insect bites and
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



infections, acne, decreased libido, decreased fertility, irregular or
i,- i,- i,- i,- i,- i,- i,- i,-



absent menstrual periods, fatigue, muscle weakness, cognitive
i,- i,- i,- i,- i,- i,- i,-



difficulties, and headaches. i,- i,-




Turner Syndrome A chromosomal disorder in females in
i,- i,-i,- i,- i,- i,- i,- i,- i,- i,-



which either an X chromosome is missing, making the person XO
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



instead of XX, or part of one X chromosome is deleted.
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-

,Tay-Sachs disease A human genetic disease caused by a
i,- i,-i,- i,- i,- i,- i,- i,- i,- i,- i,-



recessive allele that leads to the accumulation of certain lipids in
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



the brain. Seizures, blindness, and degeneration of motor and
i,- i,- i,- i,- i,- i,- i,- i,- i,-



mental performance usually become manifest a few months after
i,- i,- i,- i,- i,- i,- i,- i,- i,-



birth.


Down Syndrome i,- a condition of mild to severe intellectual i,-i,- i,- i,- i,- i,- i,- i,- i,- i,-



disability and associated physical disorders caused by an extra
i,- i,- i,- i,- i,- i,- i,- i,- i,-



copy of chromosome 21
i,- i,- i,-




Marfan Syndrome i,- i,-i,- i,- autosomal dominant trait.. i,- i,- i,-




a genetic disorder that changes the proteins that help make
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



healthy connective tissue. This leads to problems with the
i,- i,- i,- i,- i,- i,- i,- i,- i,-



development of connective tissue, which supports the bones, i,- i,- i,- i,- i,- i,- i,- i,-



muscles, organs, and tissues in your body.
i,- i,- i,- i,- i,- i,-




Marfans syndrome genetic trait type
i,- Autosomal dominant. i,- i,- i,- i,-i,- i,- i,- i,-



inherited in an autosomal pattern which means one copy of the
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



altered gene in each cell is sufficient to cause the disorder.
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-

, Viral hemorragic fevers
i,- spread by contact with infected i,- i,-i,- i,- i,- i,- i,- i,- i,-



animals or insects. Most common hosts are mosquitos, ticks,
i,- i,- i,- i,- i,- i,- i,- i,- i,-



rodents, or bats. i,- i,-




MRSA (methicillin-resistant Staphylococcus aureus)
i,- an i,- i,- i,-i,- i,- i,-



infection caused by specific bacteria that has become resistant to
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



many antibiotics i,-




B12 anemia
i,- cobalamin deficiency, is a condition that i,-i,- i,- i,- i,- i,- i,- i,- i,-



develops when your body can't make enough healthy red blood
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



cells because it doesn't have enough vitamin B12. Your body
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



needs vitamin B12 to make healthy red blood cells, white blood
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



cells, and platelets. (pernicious anemia)
i,- i,- i,- i,-




Pernicious Anemia a type of vitamin B12 anemia. An
i,- i,-i,- i,- i,- i,- i,- i,- i,- i,- i,-



autoimmune condition in which the body's immune system i,- i,- i,- i,- i,- i,- i,- i,-



attacks the actual intrinsic factor (IF) protein or the cells in the
i,- i,- i,- i,- i,- i,- i,- i,- i,- i,- i,- i,-



lining of your stomach that make it.
i,- i,- i,- i,- i,- i,-




Folate (folic acid) deficiency anemia
i,- - Folate is an essential i,- i,- i,- i,-i,- i,- i,- i,- i,- i,- i,-



vitamin for RNA and DNA synthesis within maturing RBC
i,- i,- i,- i,- i,- i,- i,- i,-




- Absorption of folate occurs in the upper small intestine
i,- i,- i,- i,- i,- i,- i,- i,- i,-

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Subido en
28 de enero de 2025
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Escrito en
2024/2025
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